OMIA:002948 : Adrenal hyperplasia, congenital, CYP21A2-related

Categories: Endocrine / exocrine gland phene (incl mammary gland)

Possible human homologues (MIM numbers): 613815 (gene) , 201910 (trait)

Cross-species summary: 21-hydroxylase deficiency in humans causes congenital adrenal hyperplasia and nonclassical hyperandrogenism.

Species in which this phene is found:
Japanese medaka (Oryzias latipes)

Edit History


  • Created by Imke Tammen2 on 30 Apr 2025
  • Changed by Imke Tammen2 on 30 Apr 2025